ClinicalTrials.gg
Not yet recruitingNCT07805239Updated Sep 4, 2026

Improve Awarness of Preeclampsia Among Pregnant Women

An observational study in Preeclampsia Awarness, sponsored by Aya Magdy Mohamed Amin. Not yet recruiting. Open to female participants aged 18 Years and older, including healthy volunteers. Per ClinicalTrials.gov, last updated 2026-09-04.

Sponsored by Aya Magdy Mohamed Amin · Observational

Study type
Observational
Model
Other
Time perspective
Cross-sectional
Enrollment
160
Ages
18 Years and older
Sex
Female
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Study summary

Preeclampsia is a major pregnancy-related hypertensive disorder and a leading cause of maternal and perinatal morbidity and mortality worldwide, particularly in developing regions. Adequate maternal awareness of preeclampsia symptoms and risk factors is crucial for early detection and timely medical intervention.

Objectives: This study aims to assess the level of awareness regarding preeclampsia, its warning signs, and its associated risk factors among pregnant women attending the antenatal care (ANC) clinic at Sohag University Hospital, and to identify socio-demographic factors associated with their awareness levels.

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Conditions studied

  • Preeclampsia Awarness

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03

In context

Pre-Eclampsia

916 studies on the registry are indexed under Pre-Eclampsia; 243 are open to participants now.

This study's planned enrollment of 160 is close to the median of 165 across 397 observational studies indexed under Pre-Eclampsia.

Browse Pre-Eclampsia studies →

Lead sponsor

This is the only study on the registry with Aya Magdy Mohamed Amin as lead sponsor.

Counted across the registry records on this site, refreshed daily.

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Who can participate

Ages eligible
18 Years and older
Sexes eligible
Female
Accepts healthy volunteers
Yes
Sampling method
Probability sample

Study population

Sohag University Hospital at the Obstetric and Gynecology department including admitted inpatient and those attending outpatient clinic .

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  1. Pregnant women aged 18 years or older.
  2. women at high risk of PE ( previous history of PE , Diabetes , chronic hypertension , kidney disease , disorders as Antiphospholipid syndrome ).
  3. Ability to communicate effectively and provide , with no cognitive or psychiatric conditions that would interfere with participation or questionnaire completion.

Exclusion criteria

Exclusion Criteria:

  1. Women with severe medical or obstetric emergencies requiring immediate management at the time of data collection.
  2. Women with cognitive impairment, severe psychiatric illness, or communication difficulties that prevent reliable completion of the questionnaire.
  3. Incomplete questionnaire responses.

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Terms in these criteria, in plain language(2)

Underlined terms in the criteria open these too. Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.

Autoimmune disease

A condition in which the immune system attacks the body’s own tissues, such as rheumatoid arthritis, lupus, psoriasis, type 1 diabetes or inflammatory bowel disease.

Immunotherapy studies often leave out active autoimmune disease, and some name exceptions, such as thyroid disease on replacement hormone. Check the exceptions this study lists.

Informed consent

Before you join, the study team explains what taking part involves — its purpose, what happens, the risks and possible benefits — and answers your questions, so you can decide freely. Consent is usually recorded on a form (the informed consent form, ICF) signed by you or, where the law allows, by someone legally authorised to decide for you.

You can keep asking questions during the study, you are told of new information that matters, and you can choose to leave at any time.

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Study design

Observational model
Other
Time perspective
Cross-sectional
Enrollment
160 participants (estimated)
Patient registry
No

Groups and cohorts

  • pregnant women

    Other: Questionnaire

Interventions

  • OtherQuestionnaire

    Data will be collected by the researcher through personal interviews with the PE admitted inpatient at the Obstetric and Gynecology department and those attending outpatient clinic at Sohag University Hospital using standardized questionnaire.

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What researchers measure

Primary outcomes

  1. Preeclampsia Knowledge score

    Assessed using an investigator-administered, validated, close-ended questionnaire covering preeclampsia awareness, risk factors, signs/symptoms, and complications. Each correct response receives 1 point, while incorrect or "don't know" responses receive 0 points. Scores are expressed as percentages and categorized into adequate knowledge (≥60%) and inadequate knowledge (\<60%).

    Time frame: Baseline (at admission to the department or attendance at the outpatient clinic)

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Study locations

No study locations are listed for this record.

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References and documents

Individual participant data

Plan to share: Undecided

No publications or documents are linked to this record.

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Timeline

Tracking since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reached

Start is estimated for Sep 2026; primary completion for Mar 2027, 6 months later.

How these figures are worked out, and which studies are left out of them.

Registered
Aug 31, 2026
First posted
Sep 4, 2026
StartEst.
Sep 1, 2026
Primary completionEst.
Mar 1, 2027
CompletionEst.
Sep 1, 2027
Last update
Sep 4, 2026
What these dates mean
Start.
When the first participant enrolled; while estimated, when the study expects to open to recruitment.
Primary completion.
When the last participant was examined or treated to collect data for the study's main question, its primary outcome. A study that stopped early gives the date its data collection stopped.
Completion.
When the last participant's last visit took place, for every outcome, secondary ones and side effects included: the end of the study. Often later than primary completion, sometimes the same day.
Actual and Est.
Actual means the registry says the date has happened. Est. (estimated) is a date the sponsor plans or expects. It can still move, and the sponsor is expected to change it to actual once it has passed.
No changes since tracking began. The registry record was last updated on Sep 4, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT07805239
Lead sponsor
Aya Magdy Mohamed Amin
Collaborators
Sohag University
Responsible party
Aya Magdy Mohamed Amin (Demonstrator of Family Medicine, Sohag University) — Sponsor-investigator
First posted
Sep 4, 2026
Start date
Sep 1, 2026 (estimated)
Primary completion
Mar 1, 2027 (estimated)
Completion
Sep 1, 2027 (estimated)
Last update
Sep 4, 2026

Study contacts

Salah Roshdy Ahmed, Professor
Contact
salahroshdy@yahoo.com
+201153008891

Oversight

FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is not yet recruiting, as verified in Sep 2026. You cannot join it, but the record below documents what was studied.

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Discussion

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